Core transcriptional regulatory circuit controlled by the TAL1 complex in human T cell acute lymphoblastic leukemia.

نویسندگان

  • Takaomi Sanda
  • Lee N Lawton
  • M Inmaculada Barrasa
  • Zi Peng Fan
  • Holger Kohlhammer
  • Alejandro Gutierrez
  • Wenxue Ma
  • Jessica Tatarek
  • Yebin Ahn
  • Michelle A Kelliher
  • Catriona H M Jamieson
  • Louis M Staudt
  • Richard A Young
  • A Thomas Look
چکیده

The oncogenic transcription factor TAL1/SCL is aberrantly expressed in over 40% of cases of human T cell acute lymphoblastic leukemia (T-ALL), emphasizing its importance in the molecular pathogenesis of T-ALL. Here we identify the core transcriptional regulatory circuit controlled by TAL1 and its regulatory partners HEB, E2A, LMO1/2, GATA3, and RUNX1. We show that TAL1 forms a positive interconnected autoregulatory loop with GATA3 and RUNX1 and that the TAL1 complex directly activates the MYB oncogene, forming a positive feed-forward regulatory loop that reinforces and stabilizes the TAL1-regulated oncogenic program. One of the critical downstream targets in this circuitry is the TRIB2 gene, which is oppositely regulated by TAL1 and E2A/HEB and is essential for the survival of T-ALL cells.

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عنوان ژورنال:
  • Cancer cell

دوره 22 2  شماره 

صفحات  -

تاریخ انتشار 2012